International safety notice
Alert 2826 (Technosurveillance) HP Bioproteses Ltda HPBIO Percutaneous Endoscopic Gastrostomy Kit Possibility of loosening the Tip and Feeding Tube components during the implant procedure.
Brazil / Anvisa · BRA · Mar 21, 2019
Key facts
| Title | Alert 2826 (Technosurveillance) HP Bioproteses Ltda HPBIO Percutaneous Endoscopic Gastrostomy Kit Possibility of loosening the Tip and Feeding Tube components during the implant procedure. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: HPBIO Percutaneous Endoscopic Gastrostomy Kit Technical Name: Gastrostomy Kit ANVISA registration number: 10166360036 Risk Class: III Affected model: PEG24 Affected serial numbers: PEG24: lot 198 to lot 199 series 01 to 50; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO HP BIOPROTESES LTDA CNPJ 54801196000142 RUA MARIA JOSÉ RANGEL 83 SÃO PAULO SP TEL 11 38537625 EMAIL MARCIAHPBIOCOMBR FABRICANTE DO PRODUTO HP BIOPROTESES LTDA RUA MARIA JOSÉ RANGEL 83 SÃO PAULO SP 04650180 BRASIL |
| Models | 10166360036, PEG24 |
| Date | Mar 21, 2019 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1